Exploring gene-environment interactions in Parkinson's diseaseMCCULLOCH, Colin C; KAY, Denise M; ZABETIAN, Cyrus P et al.Human genetics. 2008, Vol 123, Num 3, pp 257-265, issn 0340-6717, 9 p.Article

Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patientsKAY, Denise M; MORAN, Dawn; SCHELLENBERG, Gerard D et al.Annals of neurology. 2007, Vol 61, Num 1, pp 47-54, issn 0364-5134, 8 p.Article

A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9JUSTICE, Cristina M; YAGNIK, Garima; KIMONIS, Virginia et al.Nature genetics. 2012, Vol 44, Num 12, pp 1360-1364, issn 1061-4036, 5 p.Article

Postural instability/gait disturbance in Parkinson's disease has distinct subtypes: an exploratory analysisFACTOR, Stewart A; KYLE STEENLAND, N; HIGGINS, Donald S et al.Journal of neurology, neurosurgery and psychiatry. 2011, Vol 82, Num 5, pp 564-568, issn 0022-3050, 5 p.Article

Evaluation of Genes Involved in Limb Development, Angiogenesis, and Coagulation as Risk Factors for Congenital Limb DeficienciesBROWNE, Marilyn L; CARTER, Tonia C; KAY, Denise M et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 10, pp 2463-2472, issn 1552-4825, 10 p.Article

LRRK2 G2019S in families with parkinson disease who originated from europe and the middle east : Evidence of two distinct founding events beginning two millennia agoZABETIAN, Cyrus P; HUTTER, Carolyn M; ROBERTS, John W et al.American journal of human genetics. 2006, Vol 79, Num 4, pp 752-758, issn 0002-9297, 7 p.Article

Early Infantile Krabbe Disease: Results of the World-Wide Krabbe RegistryDUFFNER, Patricia K; BARCZYKOWSKI, Amy; JAIAL, Kabir et al.Pediatric neurology. 2011, Vol 45, Num 3, pp 141-148, issn 0887-8994, 8 p.Article

Parkinson's disease and LRRK2 : Frequency of a common mutation in U.S. movement disorder clinicsKAY, Denise M; ZABETIAN, Cyrus P; FACTOR, Stewart A et al.Movement disorders. 2006, Vol 21, Num 4, pp 519-523, issn 0885-3185, 5 p.Article

Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's diseaseHAMZA, Taye H; ZABETIAN, Cyrus P; KUSEL, Victoria I et al.Nature genetics. 2010, Vol 42, Num 9, pp 781-785, issn 1061-4036, 5 p.Article

Combined Effects of Smoking, Coffee, and NSAIDs on Parkinson's Disease RiskPOWERS, Karen M; KAY, Denise M; MARTINEZ, Erica D et al.Movement disorders. 2008, Vol 23, Num 1, pp 88-95, issn 0885-3185, 8 p.Article

Genetic Association Between α-Synuclein and Idiopathic Parkinson's DiseaseKAY, Denise M; FACTOR, Stewart A; ATKINS, April J et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2008, Vol 147, Num 7, pp 1222-1230, issn 1552-4841, 9 p.Article

Newborn Screening for Severe Combined Immunodeficiency in 11 Screening Programs in the United StatesKWAN, Antonia; ABRAHAM, Roshini S; BROKOPP, Charles et al.JAMA, the journal of the American Medical Association. 2014, Vol 312, Num 7, pp 729-738, issn 0098-7484, 10 p.Article

Later Onset Phenotypes of Krabbe Disease: Results of the World-Wide RegistryDUFFNER, Patricia K; BARCZYKOWSKI, Amy; KAY, Denise M et al.Pediatric neurology. 2012, Vol 46, Num 5, pp 298-306, issn 0887-8994, 9 p.Article

Disease-Related and Genetic Correlates of Psychotic Symptoms in Parkinson's DiseaseFACTOR, Stewart A; KYLE STEENLAND, N; HIGGINS, Donald S et al.Movement disorders. 2011, Vol 26, Num 12, pp 2190-2195, issn 0885-3185, 6 p.Article

SNCA Variant Associated With Parkinson Disease and Plasma α-Synuclein LevelMATA, Ignacio F; MIN SHI; KAY, Denise M et al.Archives of neurology (Chicago). 2010, Vol 67, Num 11, pp 1350-1356, issn 0003-9942, 7 p.Article

Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's diseaseZABETIAN, Cyrus P; HUTTER, Carolyn M; MONTIMURRO, Jennifer S et al.Annals of neurology. 2007, Vol 62, Num 2, pp 137-144, issn 0364-5134, 8 p.Article